AU2002353700A1 - New use for the treatment of gastroesophageal reflux disease - Google Patents
New use for the treatment of gastroesophageal reflux disease Download PDFInfo
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- AU2002353700A1 AU2002353700A1 AU2002353700A AU2002353700A AU2002353700A1 AU 2002353700 A1 AU2002353700 A1 AU 2002353700A1 AU 2002353700 A AU2002353700 A AU 2002353700A AU 2002353700 A AU2002353700 A AU 2002353700A AU 2002353700 A1 AU2002353700 A1 AU 2002353700A1
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- Prior art keywords
- receptor agonist
- cannabinoid receptor
- treatment
- prevention
- acceptable salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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Description
WO 03/043619 PCT/SEO2/02108 1 NEW USE FOR THE TREATMENT OF GASTROESOPHAGEAL REFLUX DISEASE Field of the invention 5 The present invention relates to the use of cannabinoid receptor agonists for the inhibition of transient lower esophageal sphincter relaxations. A further aspect of the invention is directed to the use of cannabinoid receptor agonists for the treatment of gastroesophageal reflux disease, as well as for the treatment of regurgitation such as regurgitation in infants, lung disease, chronic laryngitis and asthma. 10 Background of the invention The lower esophageal sphincter (LES) is prone to relaxing intermittently. As a consequence, fluid from the stomach can pass into the esophagus since the mechanical is barrier is temporarily lost at such times, an event hereinafter referred to as "reflux". Gastroesophageal reflux disease (GERD) is the most prevalent upper gastrointestinal tract disease. Current pharmacotherapy aims at reducing gastric acid secretion, or at neutralizing acid in the esophagus. The major mechanism behind reflux has been considered to depend 20 on a hypotonic lower esophageal sphincter. However, e.g. Holloway & Dent (1990) Gastroenterol. Clin. N. Amer. 19, pp. 517-535, has shown that most reflux episodes occur during transient lower esophageal sphincter relaxations (TLESRs), i.e. relaxations not triggered by swallows. It has also been shown that gastric acid secretion usually is normal in patients with GERD. 25 GERD is caused by reflux of gastric contents into the esophagus leading to heartburn and other typical symptoms. In many cases, an inflammation develops in the distal esophagus (esophagitis). It has been known for a long time that suppression of production of gastric acid ameliorates both symptoms and esophagitis. However, some patients continue to have 30 symptoms despite adequate control of acid secretion. Reflux of other noxious factors is believed to be responsible for those symptoms. Most focus has been centered on the WO 03/043619 PCT/SEO2/02108 2 importance of bile acids, and the development of severe GERD is related to the degree of esophageal bile acid exposure. Historically the term cannabinoids referred to the main components of Cannabis sativa 5 (marijuana), including about sixty molecules, but this term has been extended to also include endogenous cannabinoids and a wide variety of chemical entities which interact with the two known cannabinoid receptors, CB I and CB2. Recently, the existence of a previously unknown cannabinoid receptor subtype has been suggested (Mol. Pharmacol. (2001), 60: pp. 155-163, PNAS (1999), 96: pp. 14136-14141). The cannabinoid receptors o10 belong to the G-protein-coupled superfamily, and the CB 1 receptor is expressed predominantly in the central nervous system and to a lesser extent in peripheral tissues (Nature (1990), 346: pp. 561-564), whereas the CB2 receptor is located in the periphery and is primarily restricted to cells and tissues associated with immune functions (Nature (1993), 365: pp. 61-65). 15 There are currently four known main chemical groups of cannabinoid receptor agonists: 1) eicosanoids and their analogues, which are animal-derived cannabinoids. Anandamide is one example within this group: 0 20 Anandamide 2) classical cannabinoids and their analogues, which are plant-derived cannabinoids, such as A 9 -THC (A 9 -tetrahydrocannabinol): N1 OH
H
, 25
A'-THC
WO 03/043619 PCT/SEO2/02108 3 3) non-classical cannabinoids, such as CP 55,940, developed by Pfizer: OH OH OH ;and CP 55,940 5 4) amininoalkylindole cannabinoids such as WIN 55,212-2, developed by Sterling Winthrop: 10 O 0 (N O 0) WIN 55,212-2 The only cannabinoids having obtained drug approval so far, belong to the classical is cannabinoid family. A 9 -THC having the generic name Dronabinol, is registered in the United States under the trade mark Marinol @ , for use against nausea induced by anticancer drugs and to combat weight loss in AIDS patients by stimulating appetite. Nabilone is a synthetic derivative developed by Eli Lilly (Cesamet ), registered in Canada, UK and Eire for the suppression of nausea and vomiting provoked by cancer chemotherapy. 20 A pharmacological review on CB 1 and CB 2 receptor ligands has been disclosed by Pertwee, R.G. in Curr. Med. Chem. (1999) 6: pp.635-664. For additional comprehensive reviews see e.g. Barth F. Exp. Opin. Ther. Patents (1998) 8(3): pp. 301-313; WO 03/043619 PCT/SE02/02108 4 Pertwee, R.G. Exp. Opin. Invest. Drugs (2000) 9(7): pp.J55 3 -1 5 7 1; Goy, P.; Jagerovic, N. Exp. Opin. Ther. Patents (2000) 10(10): pp.]1529-1538, as well as references cited therein. WO 01/ 32169 of Yissum Research Development, discloses a pharmaceutical composition s for treating or preventing inter alia pain, gastrointestinal disorders, and autoimmune diseases, by the administration of specific compounds acting on the CB2 receptor. Inflammatory Bowel Disease (IBD) is one disease for which compounds disclosed therein have been tested. 10 The object of the present invention was to find a new way for the inhibition of transient lower esophageal sphincter relaxations (TLESRs), thereby preventing reflux. More particularly the object of the invention was to find a new and improved way of treating gastroesophageal reflux disease (GERD), as well as a new and improved way for the treatment of regurgitation such as regurgitation in infants, lung disease, chronic laryngitis 15 and asthma. Outline of the invention 20 It has now surprisingly been found that cannabinoid receptor agonists can be used for the inhibition of transient lower esophageal sphincter relaxations (TLESRs), and thus for the treatment of gastroesophageal reflux disease (GERD). Consequently, the present invention is directed to the use of a cannabinoid receptor agonist for the manufacture of a medicament for the inhibition of transient lower esophageal 25 sphincter relaxations (TLESRs). A further aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the prevention of reflux.
WO 03/043619 PCT/SE02/02108 Still a further aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the treatment of gastroesophageal reflux disease (GERD).Effective management of regurgitation would be an important way of preventing, as well as curing lung disease due to aspiration of regurgitated gastric contents. Thus, a 5 further aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the treatment or prevention of regurgitation. Effective management of regurgitation in infants would be an important way of preventing, as well as curing lung disease due to aspiration of regurgitated gastric contents, and for o10 managing failure to thrive, inter alia due to excessive loss of ingested nutrient. Thus, a further aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the treatment of regurgitation in infants. Another aspect of the invention is the use of a cannabinoid receptor agonist for the 15 manufacture of a medicament for the management of failure to thrive. Still a further aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the treatment or prevention of lung disease. The lung disease to be treated may inter alia be due to aspiration of regurgitated gastric contents. 20 Another aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the treatment or prevention of asthma, such as reflux related asthma. 25 A further aspect of the invention is the use of a cannabinoid receptor agonist for the manufacture of a medicament for the treatment or prevention of chronic laryngitis. A further aspect of the present invention is a method for the inhibition of transient lower esophageal sphincter relaxations (TLESRs), whereby a pharmaceutically and WO 03/043619 PCT/SE02/02108 6 pharmacologically effective amount of a cannabinoid receptor agonist is administered to subject in need of such inhibition. Another aspect of the invention is a method for the prevention of reflux, whereby a 5 pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist is administered to a subject in need of such prevention. Still a further aspect of the invention is a method for the treatment of gastroesophageal reflux disease (GERD), whereby a pharmaceutically and pharmacologically effective 10 amount of a cannabinoid receptor agonist is administered to a subject in need of such treatment. Another aspect of the present invention is a method for the treatment or prevention of regurgitation, whereby a pharmaceutically and pharmacologically effective amount of a 15is cannabinoid receptor agonist is administered to a subject in need of such treatment. Yet another aspect of the invention is a method for the treatment or prevention of regurgitation in infants, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist is administered to a subject in need of such 20 treatment. Still a further aspect of the invention is a method for the treatment, prevention or inhibition of lung disease, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist is administered to a subject in need of such treatment. The 25 lung disease to be treated may inter alia be due to aspiration of regurgitated gastric contents. Still a further aspect of the invention is a method for the management of failure to thrive, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid 30 receptor agonist is administered to a subject in need of such treatment.
WO 03/043619 PCT/SE02/02108 7 A further aspect of the invention is a method for the treatment or prevention of asthma, such as reflux-related asthma. A further aspect of the invention is a method for the treatment or prevention of chronic 5 laryngitis. A further aspect of the invention is the use of a cannabinoid receptor agonist having selectivity for the CB 1 receptor, in any one of the indications discussed above. Still a further aspect of the invention is the use of a cannabinoid receptor agonist having lo selectivity for the CB2 receptor, in any one of the indications discussed above. For the purpose of this invention, the term "agonist " should be understood as including both full agonists as well as partial agonists, whereby a "partial agonist" should be understood as a compound capable of partially, but not fully, activating cannabinoid is receptors. The wording "cannabinoid receptor agonist" as used herein, includes not only full cannabinoid receptor agonists or partial cannabinoid receptor agonists, but also includes indirect cannabinoid receptor agonists. By the wording "indirect cannabinoid receptor 20 agonist" as used herein is meant inhibitors to the enzyme fatty acid amidohydrolase (FAAH) as well as inhibitors to the enzyme anandamide transporter (ANT). Inhibitors to ANT or FAAH may be useful as indirect cannabinoid receptor agonists by increasing the concentration of endocannabinoids at the cannabinoid receptors, and thus useful for the inhibition of TLESRs. 25 The wording "TLESR", transient lower esophageal sphincter relaxations, is herein defined in accordance with Mittal, R.K., Holloway, R.H., Penagini, R., Blackshaw, L.A., Dent, J., 1995; Transient lower esophageal sphincter relaxation. Gastroenterology 109, pp. 601-610. 30 The wording "reflux" is defined as fluid from the stomach being able to pass into the esophagus, since the mechanical barrier is temporarily lost at such times.
WO 03/043619 PCT/SE02/02108 8 The wording "GERD", gastroesophageal reflux disease, is defined in accordance with van Heetrwarden, M.A., Smout A.J.P.M., 2000; Diagnosis of reflux disease. Baillire's Clin. Gastroenterol. 14, pp. 759-774. 5 The wording "regurgitation" is defined as the expulsion of undigested food and gastric juice. The wording "lung disease" is defined as any deviation from or any interruption of the 10 normal function of the lung. The wording "laryngitis" is defined as an inflammation of the larynx, a condition with dryness and soreness of the throat, hoarseness, cough and dysphagia. The wording "chronic" is defined as persisting over a long period of time. 15 Asthma is an inflammatory disorder of the airways, characterized by periodic attacks of wheezing, shortness of breath, chest tightness and coughing. The wording "reflux-related asthma" is defined in accordance with Richter, J.E. 2000; Gastroesophageal Reflux Disease and Asthma: The Two Are Directly Related. Am. J. Med. 108 (4A), pp. 153S-158S. 20 In one aspect of the invention, the cannabinoid receptor agonist(s) as used in accordance with the present invention, have an effect duration of approximately 4 to 24 hours. The wording "duration" is defined as the time period from the time of onset to the time when no effect can be measured. 25 Within the scope of the present invention is particularly the use of cannabinoid receptor agonists falling within the four main chemical categories of cannabinoid receptor agonists. Thus, eicosanoids, and analogues thereof; classical cannabinoids and analogues thereof; non-classical cannabinoids and analogues thereof; and amninoalkylindole cannabinoids and 30 analogues thereof, are particularly useful in accordance with the invention.
WO 03/043619 PCT/SE02/02108 9 Examples of specific compounds having agonistic, indirect or partial agonistic, affinity to cannabinoid (CB) receptors, thereby being useful in accordance with the invention, are the following compounds. 5 I) Eicosanoid CB receptor agonists: * Anandamide (commercially available from e.g.Tocris Cookson, Bristol, U.K.), which is a compound of the formula 0 * eicosa-5,8,11,14-tetraenoic acid (2-chloro-ethyl)-amide, also known as Arachidonyl-2'-chloroethylamide (ACEA, commercially available from e.g. Tocris Cookson, Bristol, U.K.); and 15is * eicosa-5,8,11,14-tetraenoic acid cyclopropylamide, also known as Arachidonyl cyclopropylamide (ACPA, commercially available from e.g. Tocris Cookson, Bristol, U.K.). 20 II) Classical CB receptor agonists: * A 9 -THC (A9-tetrahydrocannabinol, commercially available from e.g. Sigma Aldrich), a compound of the formula \N OH H H 0 /, having the chemical name 2s 6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-l1-ol, as well as the enantiomer (-)-A9-tetrahydrocannabinol [(-)-A 9 -THC)]; and WO 03/043619 PCT/SEO2/02108 10 (-)-(R,R)-6,6-Dimethyl-(1,1-dimethylheptyl)-l1-hydroxy-9-(hydroxymethyl) 6a,7,10,10a-tetrahydro-6H-dibenzo[b,d]pyran, [11-hydroxy-A -THC dimethylheptyl], also known as HU-210 (commercially available from e.g. Tocris Cookson, Bristol, U.K.). 5 III) Non-classical CB receptor agonists: * CP 55,940, a compound having the chemical name 5-(1,1-dimethyl-heptyl)-2-[5 hydroxy-2-(3-hydroxy-propyl)-cyclohexyl]-phenol (commercially available from 10 e.g. Tocris Cookson, Bristol, U.K.), and the chemical structure OH OH OH ;and * (-)-(6S,6aR,9R,10aR)-5,6,6a,7,8,9,10a-octahydro-6-methyl-3-[(R)-1-methyl-4 15 phenylbutoxyl]-1,9-phenanthridinediol 1-acetate, also known as L-nantradol (CP 50,556). IV) Aminoalkylindole CB receptor agonists: * WIN 55,212-2 (commercially available from e.g. Tocris Cookson, Bristol, U.K.), 20 having the chemical structure O N O N and the chemical name (2-methyl-3-morpholin-4-ylmethyl-3,4-dihydro-5-oxa-2a aza-acenaphthylen-1-yl)-naphthalen-1-yl-methanone; and WO 03/043619 PCT/SE02/02108 11 * L-768,242, having the chemical name ( 2
,
3 -dichloro-phenyl)-[5-methoxy-2-methyl 3
-(
2 -morpholin-4-yl-ethyl)-indol-l1-yl]-methanone, and the chemical structure CH O N 0 N O H 0 Cl Cl 5 Also useful in further aspects of the present invention, are cannabinoid receptor agonists disclosed in WO 01/ 31169; WO 99/ 51560; EP 0860168; WO 97/ 00860; WO 01/ 32169, such as the compound HU-308; WO 01/ 28497, such as the compound AM 1703; WO 01/ 74763; WO 01/ 29007; WO 01/ 28557. Further cannabinoid receptor 10to agonists which may be useful in accordance with the present invention are compounds disclosed in WO 97/ 29079, such as arylamides of the formula o cN \/NH2 is compounds as disclosed in WO 98/41519, such as pyrazoles of the formula o.
°
N
0 WO 03/043619 PCT/SEO2/02108 12 quinolines of the structure o ~ \ N 0 N 0NH2 compounds as disclosed in WO. 98/ 37061; and WO 00/ 10967, and more particularly s therein the arylsulphonarnide 0 O No F"I" F 0 Still further compounds which may be useful in accordance with the present invention are cannabinoid receptor agonists disclosed by F. Barth in Exp. Opin. Ther. Patents (1998) 10 8(3): pp. 301-313; and cannabinoid receptor agonists disclosed by P. Goya & N. Jagerovic in Exp. Opin. Ther. Patents (2000) 10(10):pp. 1529-1538. The above mentioned specific cannabinoid receptor agonists, as well as the cannabinoid receptor agonists disclosed in any one of the published patent applications above, are herein incorporated by reference. This list of cannabinoid receptor agonists should not in any way be regarded as an 15 exhaustive list limiting the scope of the invention. Examples of indirect cannabinoid receptor agonists useful in accordance with the present invention are the compounds AM 374 (commercially available from e.g. Calbiochem 20 Novabiochem Corporation) and AM 404 (commercially available from e.g. Tocris Cookson, Bristol, U.K.).
WO 03/043619 PCT/SEO2/02108 13 N OH 0 0 0 FN AM 374 AM 404 5 The use of pharmaceutically acceptable salts of cannabinoid receptor agonists is also within the scope of the present invention. Such salts are for example salts formed with mineral acids such as hydrochloric acid; alkali metal salts such as sodium or potassium salts; or alkaline earth metal salts such as calcium or magnesium salts. 10 The use of optical isomers of cannabinoid receptor agonists are also within the scope of the present invention. Cannabinoid receptor agonists having an asymmetric carbon atom are chiral compounds, and depending on the presence of asymmetric atoms, the cannabinoid receptor agonists may exist in the form of mixtures of isomers, particularly racemates, or in the form of pure isomers such as specific enantiomers. 15 WO 03/043619 PCT/SEO2/02108 14 Pharmaceutical formulations For clinical use, the cannabinoid receptor agonists are in accordance with the present invention suitably formulated into pharmaceutical formulations for oral administration. 5 Also rectal, parenteral or any other route of administration may be contemplated to the skilled man in the art of formulations. Thus, the cannabinoid receptor agonists are formulated with at least one pharmaceutically and pharmacologically acceptable carrier or adjuvant. The carrier may be in the form of a solid, semi-solid or liquid diluent. 10 In the preparation of oral pharmaceutical formulations in accordance with the invention, the cannabinoid receptor agonist(s) to be formulated is mixed with solid, powdered ingredients such as lactose, saccharose, sorbitol, mannitol, starch, amylopectin, cellulose derivatives, gelatin, or another suitable ingredient, as well as with disintegrating agents and lubricating agents such as magnesium stearate, calcium stearate, sodium stearyl fumarate 15is and polyethylene glycol waxes. The mixture is then processed into granules or compressed into tablets. Soft gelatine capsules may be prepared with capsules containing a mixture of the active compound or compounds of the invention, vegetable oil, fat, or other suitable vehicle for 20 soft gelatine capsules. Hard gelatine capsules may contain the active compound in combination with solid powdered ingredients such as lactose, saccharose, sorbitol, mannitol, potato starch, corn starch, amylopectin, cellulose derivatives or gelatine. Dosage units for rectal administration may be prepared (i) in the form of suppositories 25 which contain the active substance(s) mixed with a neutral fat base; (ii) in the form of a gelatine rectal capsule which contains the active substance in a mixture with a vegetable oil, paraffin oil, or other suitable vehicle for gelatine rectal capsules; (iii) in the form of a ready-made micro enema; or (iv) in the form of a dry micro enema formulation to be reconstituted in a suitable solvent just prior to administration. 30 WO 03/043619 PCT/SEO2/02108 15 Liquid preparations for oral administration may be prepared in the form of solutions, syrups or suspensions containing the active compound and the remainder of the formulation consisting of sugar or sugar alcohols, and a mixture of ethanol, water, glycerol, propylene glycol and polyethylene glycol. If desired, such liquid preparations 5 may contain colouring agents, flavouring agents, saccharine and carboxymethyl cellulose or other thickening agent. Liquid preparations for oral administration may also be prepared in the form of a dry powder to be reconstituted with a suitable solvent prior to use. Solutions for parenteral administration may be prepared as a solution of a compound of the 10 invention in a pharmaceutically acceptable solvent. These solutions may also contain stabilizing ingredients and/or buffering ingredients and are dispensed into unit doses in the form of ampoules or vials. Solutions for parenteral administration may also be prepared as a dry preparation to be reconstituted with a suitable solvent extemporaneously before use. 15 In one aspect of the present invention, the cannabinoid receptor agonist may be administered once or twice daily, depending on the severity of the patient's condition. A typical daily dose of the cannabinoid receptor agonist is within the range of from 0.1-500 mg (including 0.1 and 500 mg), such as 0.1 - 100 mg, but this will depend on various factors such as the route of administration, the age and weight of the patient as well 20 as of severity of the patient's condition.
WO 03/043619 PCT/SE02/02108 16 Biological evaluation Screening for compounds active against TLESR Adult Labrador retrievers of both genders, trained to stand in a Pavlov sling, are used. s Mucosa-to-skin esophagostomies are formed and the dogs are allowed to recover completely before any experiments are done. Motility measurement In brief, after fasting for approximately 17 h with free supply of water, a multilumen 10 sleeve/sidehole assembly (Dentsleeve, Adelaide, South Australia) is introduced through the esophagostomy to measure gastric, lower esophageal sphincter (LES) and esophageal pressures. The assembly is perfused with water using a low-compliance manometric perfusion pump (Dentsleeve, Adelaide, South Australia). An air-perfused tube is passed in the oral direction to measure swallows, and an antimony electrode monitored pH, 3 cm 15 above the LES. All signals are amplified and acquired on a personal computer at 10 Hz. When a baseline measurement free from fasting gastric/LES phase III motor activity has been obtained, placebo (0.9% NaC1) or test compound is administered intravenously (i.v., 0.5 ml/kg) in a foreleg vein. Ten min after i.v. administration, a nutrient meal (10% 20 peptone, 5% D-glucose, 5% Intralipid, pH 3.0) is infused into the stomach through the central lumen of the assembly at 100 ml/min to a final volume of 30 ml/kg. Immediately following the meal, air is insufflated at 40 ml/min. The experimental time from start of nutrient infusion to end of air insufflation is 45 min. The procedure has been validated as a reliable means of triggering TLESRs. 25 TLESRs is defined as a decrease in lower esophageal sphincter pressure (with reference to intragastric pressure) at a rate of >1 mmHg/s. The relaxation should not be preceded by a pharyngeal signal <2s before its onset in which case the relaxation is classified as swallow induced. The pressure difference between the LES and the stomach should be less than 30 2 mmHg, and the duration of the complete relaxation longer than 1 s.
WO 03/043619 PCT/SE02/02108 17 EXAMPLES Example 1 The aminoalkylindole cannabinoid WIN 55,212-2, purchased from Tocris Cookson 5 (Bristol, U.K.), was tested on Adult Labrador retrievers of both genders in accordance with the test model described above. Inhibition of the number of TLESRs was calculated with regard to the five preceding control experiments for each dog, and the results as set out in Table 1 below were o10 achieved. Table 1 COMPOUND DOSE [mg/kg ] % INHIBITION +SEM (N) 20+18 (4) WIN 55,212-2 0.003 70+10 (4) WIN 55,212-2 0.01 82+1 (4) WIN 55,212-2 0.03 N= number of dogs tested.; SEM=Standard Error of Mean 15 WO 03/043619 PCT/SE02/02108 18 Example 2 The aminoalkylindole cannabinoid L-768,242 was synthesized at AstraZeneca R&D M61ndal, Sweden, according to the procedure described in Bioorg. & Med. Chem. Lett. (1996); Vol. 6, No. 19, pp. 2263-2268, and tested as in Example I above. Inhibition of the number of TLESRs was calculated with regard to the five preceding control experiments for each dog, and the results as set out in Table 2 below were achieved. 10 Table 2 COMPOUND DOSE [pmolig] % INHIBITION+SEM (N) L-768,242 0.3 8 +21 (4) L-768,242 1 44 +6 (5) L-768,242 5 63 5 (4) L-768,242 7 76 +12(3) N= number of dogs tested.; SEM=Standard Error of Mean WO 03/043619 PCT/SE02/02108 19 Example 3 The pyrazole SR141716A (CB I antagonist) was synthesized at AstraZeneca R&D M61ndal, Sweden, according to the procedure described in J. Chem. Soc., Chemn. Commun. (1995); No. 15, pp 1549-1560, and tested as in Example 1 above. 5 Stimulation of the number of TLESRs was calculated with regard to the five preceding control experiments for each dog, and the results as set out in Table 3 below were achieved. 10 Table 3 COMPOUND DOSE [pmol/kg] % STIMULATION+SEM (N) SR141716A 0.22 43±16 (6) N= number of dogs tested.; SEM=Standard Error of Mean The results in the example 3 above, indicate a tonic activity of endocannabinoids mediating suppression of TLESRs, which in turn suggest that indirect cannabinoid agonists 15 (inhibitors of FAAH and ANT) are useful for the inhibition of TLESRs, and thus for treatment of GERD. The results shown in the Examples 1-3 above, indicate that cannabinoid receptor agonists are useful for the inhibition of TLESRs, and thus for the treatment of GERD. 20 25
Claims (36)
1. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for the inhibition of s transient lower esophageal sphincter relaxations (TLESRs).
2. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for the treatment of gastroesophageal reflux disease (GERD). 10
3. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for the prevention of reflux. 15is
4. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for the treatment of, or prevention of, regurgitation.
5. Use according to claim 4, wherein the regurgitation to be treated or prevented is 20 regurgitation in infants.
6. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for the treatment of, or prevention of, lung disease. 25
7. Use according to claim 6, wherein the lung disease is due to aspiration of regurgitated gastric contents. WO 03/043619 PCT/SE02/02108 21
8. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for managing failure to thrive. 5
9. Use according to claim 8, wherein the failure to thrive is due to excessive loss of ingested nutrient.
10. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, for the manufacture of a medicament for the treatment of, 10 or prevention of, asthma.
11. Use according to claim 10, wherein the asthma is reflux-related asthma.
12. Use of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an 15 optical isomer thereof, for the manufacture of a medicament for the treatment of, or prevention of, chronic laryngitis.
13. Use according to any one of claims 1-12, wherein the cannabinoid receptor agonist is a CB 1 receptor selective cannabinoid receptor agonist. 20
14. Use according to any one of claims 1-12, wherein the cannabinoid receptor agonist is a CB2 receptor selective cannabinoid receptor agonist.
15. Use according to any one of the preceding claims, wherein the cannabinoid 25 receptor agonist is an eicosanoid.
16. Use according to any one of claims 1-14, wherein the cannabinoid receptor agonist is a classical cannabinoid. WO 03/043619 PCT/SE02/02108 22
17. Use according to any one of claims 1-14, wherein the cannabinoid receptor agonist is a non-classical cannabinoid.
18. Use according to any one of claims 1-14, wherein the cannabinoid receptor 5 agonist is an aminoalkylindole cannabinoid.
19. Use according to claim 15, wherein the cannabinoid receptor agonist is selected from Anandamide; Arachidonyl-2'-chloroethylamide (ACEA); and Arachidonyl cyclopropylamide (ACPA). 10
20. Use according to claim 16, wherein the cannabinoid receptor agonist is A 9 -tetrahydrocannabinol (A 9 -THC); or 11-hydroxy-A 5 -THC-dimethylheptyl ( HU-210). 15
21. Use according to claim 17, wherein the cannabinoid receptor agonist is CP,55940: OH OH OH or L-nantradol (CP 50,556): (-)-(6S,6aR,9R, 10aR)-5,6,6a,7,8,9,10a-octahydro-6 methyl-3-[(R)- 1-methyl-4-phenylbutoxyl]-1,9-phenanthridinediol 1-acetate 20
22. Use according to claim 18, wherein the cannabinoid receptor agonist is WIN 55,212-2: 0 N 0 WO 03/043619 PCT/SE02/02108 23 or L-768,242: CH 0 0N N CH 3 Cl tY.
23. Use according to any one of claims 1-22 wherein the daily dose of the 5 cannabinoid receptor agonist is within the range of from 0.1-500 mg.
24. A method for the inhibition of transient lower esophageal sphincter relaxations (TLESRs), whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an o10 optical isomer thereof, is administered to a subject in need of such inhibition.
25. A method for the treatment of gastroesophageal reflux disease (GERD), whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer 15 thereof, is administered to a subject in need of such treatment.
26. A method for the prevention of reflux, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, is administered to a 20 subject in need of such prevention.
27. A method for the treatment of, or prevention of, regurgitation, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, 25 is administered to a subject in need of such treatment or prevention. WO 03/043619 PCT/SEO2/02108 24
28.. A method according to claim 27, wherein the regurgitation to be treated or prevented is regurgitation in infants.
29. A method for the prevention of, or treatment of, lung disease, whereby a 5 pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, is administered to a subject in need of such treatment or prevention.
30. A method according to claim 29, wherein the lung disease is due to aspiration of 10 regurgitated gastric contents.
31. A method for managing failure to thrive, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, is administered to a 15 subject in need of such management.
32. A method according to claim 31, wherein the failure to thrive is due to excessive loss of ingested nutrient. 20
33. A method for the treatment of, or prevention of, asthma, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, is administered to a subject in need of such treatment or prevention. 25
34. A method according to claim 33, wherein the asthma is reflux-related asthma.
35. A method for the treatment of, or prevention of, chronic laryngitis, whereby a pharmaceutically and pharmacologically effective amount of a cannabinoid receptor agonist, or a pharmaceutically acceptable salt or an optical isomer thereof, 30 is administered to a subject in need of such treatment or prevention. WO 03/043619 PCT/SE02/02108 25
36. A method according to any one of claims 24-35 wherein the daily dose of the cannabinoid receptor agonist is within the range of from 0.1-500 mg. 510 10
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PCT/SE2002/002108 WO2003043619A1 (en) | 2001-11-23 | 2002-11-20 | New use for the treatment of gastroesophageal reflux disease |
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WO2005039550A2 (en) * | 2003-10-24 | 2005-05-06 | Solvay Pharmaceuticals Gmbh | Novel medical uses of compounds showing cb1-antagonistic activity and combination treatment involving said compounds |
WO2005060971A1 (en) * | 2003-12-18 | 2005-07-07 | Astrazeneca Ab | Treatment of reflux-related diseases |
SE0303490D0 (en) * | 2003-12-19 | 2003-12-19 | Astrazeneca Ab | New use V |
JP2008517976A (en) | 2004-10-25 | 2008-05-29 | ゾルファイ ファーマスーティカルズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | A pharmaceutical composition for the treatment of diabetes mellitus type 1, obesity and related symptoms, comprising a CB1 cannabinoid receptor antagonist and a potassium channel opener |
CN101132781A (en) * | 2004-12-09 | 2008-02-27 | 茵西斯医疗公司 | Room-temperature stable dronabinol formulations |
US20080112895A1 (en) * | 2006-08-04 | 2008-05-15 | Insys Therapeutics Inc. | Aqueous dronabinol formulations |
WO2009020666A1 (en) * | 2007-08-06 | 2009-02-12 | Insys Therapeutics Inc. | Oral cannabinoid liquid formulations and methods of treatment |
EP2205240A1 (en) | 2007-10-02 | 2010-07-14 | Ariel-University Research And Development Company, Ltd. | Endocannabinoids for enhancing growth and development in infants |
US20090208588A1 (en) * | 2008-02-19 | 2009-08-20 | Roger Wayne Brown | GERD carbohydrate compositions |
CN103588672A (en) * | 2013-10-28 | 2014-02-19 | 史克勇 | Drug for treating cancer pain |
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CA2340445A1 (en) | 1998-05-04 | 1999-11-11 | The University Of Connecticut | Novel analgesic and immunomodulatory cannabinoids |
AU776414B2 (en) | 1998-05-29 | 2004-09-09 | Neurosciences Research Foundation, Inc. | Control of pain with endogenous cannabinoids |
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